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MilliporeSigma

T9517

Glyceryl trilinoleate

≥98% (TLC), liquid

Synonym(s):

TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)), 1,2,3-Tri-(cis,cis-9,12-octadecadienoyl)glycerol, 1,2,3-Trilinoleoylglycerol, Glycerol trilinoleate, Trilinolein

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50 MG

$46.42

100 MG

$70.12

500 MG

$117.00

1 G

$223.00

5 G

$767.00

$46.42

List Price$61.90Save 25%

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About This Item

Empirical Formula (Hill Notation):
C57H98O6
CAS Number:
Molecular Weight:
879.38
Beilstein/REAXYS Number:
1718698
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25

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biological source

synthetic (organic)

Quality Level

assay

≥98% (TLC)

form

liquid

density

0.925 g/mL at 20 °C (lit.)

functional group

ester

lipid type

neutral glycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC

InChI

1S/C57H98O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h16-21,25-30,54H,4-15,22-24,31-53H2,1-3H3/b19-16-,20-17-,21-18-,28-25-,29-26-,30-27-

InChI key

HBOQXIRUPVQLKX-BBWANDEASA-N

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1 of 4

This Item
T7752T651392860
biological source

synthetic (organic)

biological source

synthetic (organic)

biological source

Linum usitatissimum oil

biological source

plant, synthetic

functional group

ester

functional group

ester

functional group

ester

functional group

ester

assay

≥98% (TLC)

assay

-

assay

≥97% (TLC)

assay

≥97.0% (TLC)

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

shipped in

ambient

shipped in

ambient

shipped in

dry ice

shipped in

-

form

liquid

form

liquid

form

liquid

form

liquid

Application


  • Gum Arabic-Stabilized Ferric Oxyhydroxide Nanoparticles for Efficient and Targeted Intestinal Delivery of Bioavailable Iron.: This research explores the use of glyceryl trilinoleate in stabilizing nanoparticles for targeted iron delivery, highlighting its potential in improving bioavailability and therapeutic efficiency (Li et al., 2023).

Packaging

Sealed ampule.

hcodes

Hazard Classifications

Aquatic Chronic 4

Storage Class

10 - Combustible liquids

wgk_germany

awg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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Ming-Jun Gao et al.
The Plant cell, 21(1), 54-71 (2009-01-22)
The seed maturation program is repressed during germination and seedling development so that embryonic genes are not expressed in vegetative organs. Here, we describe a regulator that represses the expression of embryonic seed maturation genes in vegetative tissues. ASIL1 (for
Pei-Yu Chou et al.
The American journal of Chinese medicine, 39(4), 803-815 (2011-07-02)
Trilinolein has been identified as one of the active constituents isolated from Panax notoginseng used widely in traditional Chinese medicine. Protective actions of Panax notoginseng against cerebral ischemia, beneficial effects on the cardiovascular system, and hemostatic, antioxidant, hypolipidemic, hepatoprotective, renoprotective
Shi-Chung Chen et al.
Planta medica, 71(6), 525-529 (2005-06-23)
Trilinolein, isolated from the traditional Chinese herb Sanchi ( Panax notoginseng), has been shown to have myocardial protective effects via its antioxidant ability. However, the cellular and molecular mechanisms of the protective effect of trilinolein in the heart remain to
P J Moate et al.
Journal of dairy science, 91(2), 731-742 (2008-01-26)
Previous investigations into ruminal lipolysis of triacylglycerol and ruminal biohydrogenation (BH) of unsaturated long-chain fatty acids have generally quantified these processes with either zero-order or first-order kinetics. This investigation examined if Michaelis-Menten and other nonlinear kinetics might be useful for
Hung-Yu Yang et al.
Naunyn-Schmiedeberg's archives of pharmacology, 372(2), 160-167 (2005-09-27)
Trilinolein, isolated from the traditional Chinese herb Sanchi (Panax notoginseng), has been shown to have myocardial protective effects via its antioxidant ability. However, the cellular and molecular mechanisms of the protective effect of trilinolein in the heart remain to be

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